Home NDC 11559-057 RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20
Product NDC 11559-057
11-digit product format 115590057
Labeler code 11559
Product ID 11559-057_471eb781-3a3c-fdfa-e063-6294a90a4662
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE and TITANIUM DIOXIDE
Dosage form LIQUID
Route TOPICAL
Labeler ESTEE LAUDER INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-15
Substance OCTINOXATE; TITANIUM DIOXIDE
Active strength 22; 14 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 22 mg/mL TITANIUM DIOXIDE 14 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11559-057-01 RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 30 mL in 1 TUBE LIQUID 30 9 11559-057-01 RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 1 in 1 CARTON LIQUID 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11559-057 RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 (OCTINOXATE AND TITANIUM DIOXIDE) LIQUID [ESTEE LAUDER INC] 8 Current NDC, Legacy NDC, 2 package rows 20240131_897b8edb-f089-4a49-baca-e05806b0a068.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 45 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11559-057-01 11559005701 1 TUBE in 1 CARTON (11559-057-01) / 30 mL in 1 TUBE 1 tube 2019-07-15 0000-00-00 No No Current